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Kinetic study of the photocatalytic oxidation of ethylene over TiO2 thin films

机译:TiO2薄膜乙烯光催化氧化的动力学研究

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The photocatalytic oxidation process has been recognized as an environmental friendly,sustainable and low-cost technology for air treatment.A photocatalytic batch reactor has been employed to assess the kinetics of the oxidation of ethylene (C2H4) over immobilized titanium dioxide (TiO2) and the effect of initial pollutant concentration on the kinetics.The rate model based on the simplified mono-molecular Langmuir-Hinshelwood (LH) kinetic model was found to represent the degradation satisfactorily,however with numerical constrains.These were overcome by employing two different approaches.On one hand the Langmuir-Hinshelwood model was solved by means of the Lambert W-function and on the other hand it was reduced to a pseudo-first order rate law,both resulting in a good fit to the experimental data,thus proving that the photodegradation of C2H4 over TiO2 can be modelled by a first order rate law under low concentration conditions.Moreover,both models give a linear dependence between the reaction rate and the initial C2H4 concentration,making an estimation of reaction rate as a function of concentration possible,for a larger interval of C2H4 concentrations.
机译:光催化氧化过程已被认为是一种环保,可持续和低成本的空气处理技术。已经采用光催化批量反应器来评估乙烯(C2H4)氧化在固定化二氧化钛(TiO 2)上的动力学和初始污染物浓度对动力学的影响。发现基于简化单分子朗米尔 - 欣尔伍德(LH)动力学模型的速率模型代表了令人满意的降解,然而具有数值约束。通过采用两种不同的方法克服了这些。一只手通过兰伯特W函数解决了Langmuir-Hinshelwood模型,另一方面,它减少到伪第一阶法律,两者都符合实验数据的良好拟合,从而证明了光降解在TiO 2上的C2H4可以通过低浓度条件下通过一阶率定律进行建模.OROOVER,两种模型都在依赖于之间的线性依赖反应速率和初始C 2 H 4浓度,作为浓度的函数估计反应速率,对于较大的C 2 H 4浓度。

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